Status:

COMPLETED

Acupressure Wristbands or Standard Care in Controlling Nausea Caused by Chemotherapy

Lead Sponsor:

University of Manchester

Conditions:

Anxiety Disorder

Nausea and Vomiting

Eligibility:

All Genders

16+ years

Phase:

PHASE3

Brief Summary

RATIONALE: Acupressure wristbands may prevent or reduce nausea caused by chemotherapy. It is not yet known whether acupressure wristbands are more effective than standard care in controlling acute and...

Detailed Description

OBJECTIVES: Primary * To assess the clinical effectiveness of self-acupressure using wristbands in addition to standard care in the management of chemotherapy-induced (acute and delayed) nausea comp...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Diagnosis of any cancer
  • Scheduled to receive their first chemotherapy course
  • Scheduled to receive highly, moderately, or low-emetogenic chemotherapy
  • Scheduled to receive a chemotherapy regimen given as a single administration at the beginning of the course repeated in 3-week courses
  • Currently receiving adjuvant chemotherapy as outpatient
  • Acupressure wristband-naïve (in terms of never having tried such a wristband; may have seen or heard about such wristbands)
  • PATIENT CHARACTERISTICS:
  • Able to perform self care (i.e., no inability to use wristbands appropriately or mental incapacity preventing continuous and optimal use of wristbands) as judged by the investigators
  • No liver disease
  • No metabolic risk factors for nausea (i.e., electrolyte imbalances causing nausea/vomiting)
  • No mechanical risk factors for nausea (i.e., intestinal obstruction)
  • No nausea and/or vomiting due to use of opioids
  • No lymphedematous arms
  • No chronic alcohol use
  • PRIOR CONCURRENT THERAPY:
  • No concurrent radiotherapy
  • No concurrent chemotherapy regimens as inpatients

Exclusion

    Key Trial Info

    Start Date :

    November 1 2008

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    October 1 2010

    Estimated Enrollment :

    699 Patients enrolled

    Trial Details

    Trial ID

    NCT00978185

    Start Date

    November 1 2008

    End Date

    October 1 2010

    Last Update

    August 26 2013

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University of Manchester

    Manchester, England, United Kingdom, M13 9PL

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